Canonical Allele Identifier: CA626456456

Gene: ZNF652-AS1

Linked Data

• dbSNP Id: rs1441757557
• gnomAD v2: 17-47440534-C-T
• gnomAD v3: 17-49363172-C-T
• gnomAD v4: 17-49363172-C-T
• MyVariant Identifiers: chr17:g.47440534C>T (hg19) ; chr17:g.49363172C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49363172C>T , CM000679.2:g.49363172C>T	GRCh38
NC_000017.10:g.47440534C>T , CM000679.1:g.47440534C>T	GRCh37
NC_000017.9:g.44795533C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110882.1:n.136+655C>T
NR_110883.1:n.31-1107C>T
NR_110884.1:n.58-1107C>T